HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 14085931, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-(Trifluoromethyl)phenol | HCID 67874 | — |
| Catalyst | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14085931 | HCID 14085931 | 51.3% |
Reaction Steps
4-(Trifluoromethyl)phenol (1.50 g, 9.25 mmol), allyl bromide (14.55 9, 12.03 mmol), Cs2CO3 (3.62 g, 11.10 mmol), and water (15 drops) were combined in DMF (40 mL) and the mixture stirred for 12 h. The reaction mixture was then concentrated under reduced pressure, diluted with water, and extracted with EtOAc (2×). The combined organic phases were dried over Na2SO4, filtered, and concentrated under reduced pressure to give 0.96 g (51%) of thetitle compound as a light-yellow oil. 1H NMR (400 MHz, CDCl3): δ 4.59 (d, 2H), 5.32 (d, 1H), 5.43 (d, 1 H), 6.05 (m, 1H), 6.97 (d, 2H), 7.53 (d, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07714004B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-b0fc47a9486643c399eb0e20a63e4e9d |
| Source note | uspto-grants-2010_05 |